This intermediate provides the essential isoxazole ring system that forms a core structural component of Leflunomide. During the synthesis, it undergoes conversion into the corresponding amide and is further transformed through cyclization and functional-group modifications to build the final active molecule. Its defined heterocyclic framework and reactivity make it crucial for ensuring an efficient, reliable, and high-purity synthetic route to Leflunomide. 5-Methylisoxazole-4-carboxylic acid is a key starting intermediate employed to synthesize Leflunomide, an immunomodulatory drug for rheumatoid arthritis.
5-Methylisoxazole-4-carboxylic acid
| API Name | Leflunomide |
|---|---|
| CAS No | 42831-50-5 |
| Molecular Formula | C5H5NO3 |
| Molecular Weight | 127.10 g/mol |
| Synonyms | 5-methyl-1,2-oxazole-4-carboxylic acid |
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Frequently Asked Questions
This intermediate provides the essential isoxazole ring system that forms a core structural component of Leflunomide. During the synthesis, it undergoes conversion into the corresponding amide and is further transformed through cyclization and functional-group modifications to build the final active molecule. Its defined heterocyclic framework and reactivity make it crucial for ensuring an efficient, reliable, and high-purity synthetic route to Leflunomide. 5-Methylisoxazole-4-carboxylic acid is a key starting intermediate employed to synthesize Leflunomide, an immunomodulatory drug for rheumatoid arthritis.
The CAS number of 5-Methylisoxazole-4-carboxylic acid is 42831-50-5.
The molecular formula of 5-Methylisoxazole-4-carboxylic acid is C5H5NO3.
The listed molecular weight of 5-Methylisoxazole-4-carboxylic acid is 127.10 g/mol.
5-Methylisoxazole-4-carboxylic acid is listed as being used in connection with the following API: Leflunomide.
The listed synonym or IUPAC name for 5-Methylisoxazole-4-carboxylic acid is 5-methyl-1,2-oxazole-4-carboxylic acid.